Results 111 to 120 of about 183,560 (141)
Effects of macromolecular crowding on intracellular diffusion from a single particle perspective. [PDF]
Biophys Rev, 2010 Hall D, Hoshino M.
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The 4,755 Wilf-equivalence classes of permutations of length eight
Vatter's Question 3.1 asks how many Wilf-equivalence classes of length-eight permutations exist. Alex Dobner answered the question in a personal note posted in March 2026: there are exactly 4,755 classes. This deposit is an independent, fully audited confirmation and citable record: the paper (PDF) plus the complete machine-readable certificate archive
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Detection and integration of genotyping errors in statistical genetics. [PDF]
Am J Hum Genet, 2002 Sobel E, Papp JC, Lange K.
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Algorithm-assisted discovery of an intrinsic order among mathematical constants. [PDF]
Proc Natl Acad Sci U S AElimelech R +8 more
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RNA structures with pseudo-knots: graph-theoretical, combinatorial, and statistical properties. [PDF]
Bull Math Biol, 1999 Haslinger C, Stadler PF.
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Marker pair selection for mapping quantitative trait loci. [PDF]
Genetics, 2001 Piepho HP, Gauch HG.
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Anion inhibitor-sensitive unidirectional sodium movements in the human erythrocyte. [PDF]
J Gen Physiol, 1978 Callahan TJ, Goldstein DA.
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Families of Shape-Wilf-Equivalent Claw-Shaped Partially Ordered Patterns
Partially ordered patterns (POPs) generalize classical permutation patterns and have been extensively studied in the contexts of permutations, words, compositions, and partitions. Burstein, Han, Kitaev, and Zhang established the shape-Wilf-equivalence for individual claw-shaped POPs.
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